Evidence map›Paper›PMID 34910584›Full record

ArticleMolecular biology of the cell2022

A multiparametric activity profiling platform for neuron disease phenotyping and drug screening.

Bruno Boivin, Kasper C D Roet, Xuan Huang, Kyle W Karhohs, Mohammad H Rohban, Jack Sandoe, Ole Wiskow, Rie Maeda, Alyssa Grantham, Mary K Dornon and 6 more

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Bruno BoivinF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Kasper C D RoetF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Xuan HuangF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Kyle W KarhohsBroad Institute of Harvard and MIT, Imaging Platform, Cambridge, MA 02142.
Mohammad H RohbanBroad Institute of Harvard and MIT, Imaging Platform, Cambridge, MA 02142.
Jack SandoeDepartment of Stem Cell and Regenerative Biology, Harvard Stem Cell Institute, Cambridge, MA 02138.
Ole WiskowDepartment of Stem Cell and Regenerative Biology, Harvard Stem Cell Institute, Cambridge, MA 02138.
Rie MaedaF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Alyssa GranthamF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Mary K DornonF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Jenny ShaoF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Devlin FrostF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.
Dylan BakerDepartment of Stem Cell and Regenerative Biology, Harvard Stem Cell Institute, Cambridge, MA 02138.
Kevin EgganDepartment of Stem Cell and Regenerative Biology, Harvard Stem Cell Institute, Cambridge, MA 02138.
Anne E CarpenterBroad Institute of Harvard and MIT, Imaging Platform, Cambridge, MA 02142.
Clifford J WoolfF. M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115.

Funding

Unravelling Mechanisms and Novel Therapeutic Targets for Peripheral Neuropathy and Neuropathic Pain (Diversity Supplement)R35NS105076 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI WOOLF, CLIFFORD J · 2018 to 2025
$9.5M
Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI SCOTT Loren POMEROY, MUSTAFA SAHIN · 2021 to 2026
$9.4M
Extracting rich information from biological imagesR35GM122547 · NIGMS · BROAD INSTITUTE, INC. · PI Anne E. Carpenter · 2017 to 2026
$6.2M
NICHD NIH HHS P50 HD105351NIGMS NIH HHS R35 GM122547NINDS NIH HHS R35 NS105076
6 · The paper itself

Abstract

Patient stem cell-derived models enable imaging of complex disease phenotypes and the development of scalable drug discovery platforms. Current preclinical methods for assessing cellular activity do not, however, capture the full intricacies of disease-induced disturbances and instead typically focus on a single parameter, which impairs both the understanding of disease and the discovery of effective therapeutics. Here, we describe a cloud-based image processing and analysis platform that captures the intricate activity profile revealed by GCaMP fluorescence recordings of intracellular calcium changes and enables the discovery of molecules that correct 153 parameters that define the amyotrophic lateral sclerosis motor neuron disease phenotype. In a high-throughput screen, we identified compounds that revert the multiparametric disease profile to that found in healthy cells, a novel and robust measure of therapeutic potential quite distinct from unidimensional screening. This platform can guide the development of therapeutics that counteract the multifaceted pathological features of diseased cellular activity.

Indexed as

Amyotrophic Lateral SclerosisDrug DiscoveryDrug Evaluation, PreclinicalHumansNeuronsPhenotype

Identifiers

PMID34910584
PMCPMC9265164

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.